Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005632276

FEI Number

3005632276

Entity Name

LEINA-WERKE GMBH

City/State/Country

WINDECK North Rhine-Westphalia, DE

Establishment Address

MAUELER FELD 1, WINDECK North Rhine-Westphalia 51570, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LEINA-WERKE GMBH (Owner Number: 9084068)

Owner / Operator Contact Address

MAUELER FELD 1, --, WINDECK, NRW, DE-NW 51570, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

First aid kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2013-11-13

Official Correspondent

Philipp Stockmann

US Agent Details

Sebastian Feye Business: Accurate Consultants Inc Email: Sebastian@accuratefdaconsulting.com Phone: (619) 5171762

Related Public Records

Same Entity

LEINA-WERKE GMBH

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005632276. Last updated year: 2026. Please use registration number 3005632276 when referencing this establishment in official correspondence.